Purpose:
- To demonstrate that the process has the capability to produce products that consistently meet all drawing requirements and specifications at the requested production rate and to reduce product/process risks.
- To ensure that the supplier can successfully meet this requirement on time before SOP (Start of Production) Veoneer requires:
- First-Production-Trial-Run
- PPAP-Production-Trial-Run
- Run at Rate
- To ensure, that the supplier can submit PPAP (Production Part Approval Process) on time, complete and "right the first time“ the First Production-Trial-Run and implementation of resulting corrective actions before PPAP-Production-Trial-Run is required.
- Any deviation from the following rules/requirements needs a project specific approval by Veoneer.
Input from Veoneer:
- SQPS-412 (Interim Inspection Plan)
Requirements:
Depending on the defined "SQPS-927 CLD3 GUIDELINES":
- CLD 1 : Production-Trial-Runs and documentation is mandatory.
- CLD 2 : Production-Trial-Runs and documentation is mandatory and to be submitted.
- CLD 3 : as CLD 2 plus Veoneer participation at supplier's Production-Trial-Runs including Go & See PFMEA activities.
- The "SQPS-925 Production Trial Run Standard" lines out the timing requirements, the demanded Production-Trial-Run content, conditions and documentation.
- The length of time between the trials should be considered in the project time plan and included in the S-APQP (from project start on) and provide adequate time for correction of deviations. The time length is defined supplier-, project-, and process specific and shall be integrated into the SQP project (see Training) by the Supplier Quality Engineer.
- Any deviations must result in an approved action plan supporting the project time line.
- If the First-Production-Trial is done under serial production conditions and the results meet the PPAP-requirements, these results can be used for the PPAP-Production-Trial-Run and for PPAP-submission. The decision to skip the PPAP-Production-Trial-Run or any of its contents, may only be taken after the First Production-Trial-Run has been executed as scheduled and the actual results confirm such decision.
- If the PPAP-Production-Trial-Run (according to Production-Trial-Run-Standard) satisfies the Run at Rate requirements, the PPAP Production-Trial can be counted as a Run at Rate in agreement with Veoneer.
- Parts produced in the Production-Trial-Runs are manufactured at suppliers risk. If parts are at PPAP-approved engineering level, they can be sold.
All parts ordered from Production-Trial-Runs shall be sold at serial price.
Output from Supplier:
For CLD 2 and CLD 3:
- measure and document all drawing and specification characteristics
- conduct a capability-study (reference: VS052)
- conduct and document a process quality audit (use "SQPS-914 Production Trial Run Checklist")
- conduct and document a production capacity evaluation (use SQPS-913 Production Trial Capacity Report) according to the agreed project time line.
Required Documents:
- Dimensional-Report (use AIAG-manual form), optional use Veoneer-form : "SQPS-907 Dimensional Report"
- Capability Study: No specific form required.
- SQPS-914 Production Trial Run Checklist
- SQPS-913 Production Trial Capacity Report
Reference Documents:
- SQPS-925 Production Trial Run Standard
- AIAG-Manual APQP
- AIAG-Manual PPAP
- VS052 (Product Characteristics Classification)
- VS104 FMEA
- SQPS-927 CLD3 GUIDELINES
- SQPS-918 S-APQP Overview